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Myderm pro freeze cooling menthol pain relief roll-on - Medication Information

Product NDC Code 72667-073
Drug Name

Myderm pro freeze cooling menthol pain relief roll-on

Type Brand
Active Ingredients
Menthol 6 g/100g
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 415976
Application Number M017
Labeler Name Inspec Solutions
Packages
Package NDC Code Description
72667-073-01 89 g in 1 bottle, plastic (72667-073-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Menthol 6%

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Direction: Apply to affectered area not more that 3 to 4 times daily.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredient Aloe Barbadensis Leaf Juice Arctium Lappa Root Extract Arnica Montana Flower Extract Boswellia Carterii resin Extract Calendula Officinalis Extract Camellia Sinensis Leaf Extract Camphor Carbomer FD & C Blue #1 FD & C Yellow #5 Glycerin Isopropyl Alcohol Isopropyl Myristate llex Paraguariensis Leaf Extract Melissa Officinalis Leaf Extract Phenoxyethanol Silicon dioxide Tocopheryl Acetate Triethanolamine Water

Purpose

Information about the drug product’s indications for use.
Menthol 6%------------------------------------------------------------Topical Analgesic

Spl product data elements

Usually a list of ingredients in a drug product.
MyDerm Pro Freeze Cooling Menthol Pain Relief Roll-On Menthol GREEN TEA LEAF CAMPHOR, (-)- CALENDULA OFFICINALIS FLOWER FRANKINCENSE FD&C YELLOW NO. 5 ARNICA MONTANA FLOWER CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE GLYCERIN ISOPROPYL ALCOHOL PHENOXYETHANOL .ALPHA.-TOCOPHEROL ACETATE MENTHOL MENTHOL FD&C BLUE NO. 1 ISOPROPYL MYRISTATE ILEX PARAGUARIENSIS LEAF MELISSA OFFICINALIS LEAF SILICON DIOXIDE TROLAMINE ALOE VERA LEAF ARCTIUM LAPPA ROOT

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
MyDerm Freeze

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
keep out of reach of children if swallowed,get medical help or contact a poson Control Center Immediately.

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask doctor if condition worsens, or if symtoms persist for more than 7 days, or clean up and reoccur again within a few days.

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product avoid contacts with the eyes or mucous membranes. do not apply to wounds or damaged skin. do not apply to irritated skin. do not bandage. wash hands after use with cool water. do not use with heating pad or device.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
For external use only.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API